TMC-ACTREC Scientific Officer Job

TMC-ACTREC Scientific Officer Job For PhD Biochem & Immunology

TMC-ACTREC Scientific Officer Job For PhD Biochem & Immunology. PhD candidates with relevant experience are encouraged to attend an interview for the Scientific Officer vacancy. ACTREC is hiring PhD Biochem & Immunology. Interested candidates can check out all of the details below:

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TATA MEMORIAL CENTRE
ADVANCED CENTRE FOR TREATMENT, RESEARCH AND
EDUCATION IN CANCER (ACTREC)
(A Grant-in-Aid Institution of the Department of Atomic Energy, Government of India)

No. ACTREC/Advt.24/2021

ONLINE INTERVIEW FOR AD-HOC SCIENTIFIC OFFICER ‘D’ (CAR T Cell Therapy Centre) ON CONTRACT BASIS
Date: 11th May 2021 (Tuesday)
Time: 03:30 p.m. to 04:30 p.m.

Position: Scientific Officer ‘D’ (CAR T Cell Therapy Centre)

Vacancies: 01

Duration: 6 months as well as is extendable.

How to Apply for ACTREC Vacancy:

Interested Applicants may register for a video interview (with zoom) by sending a request email to [email protected] mentioning the post applied for, in the subject line.
For queries, Applicants may contact 91-22-68735000 or 91-22-68735000 (Extn-5557).

Qualification & Experience:

PhD in Biochemistry/Immunology with a minimum of 3 years experience in CART Cell Therapy, GMP grace Clinical manufacturing of Cell Therapy Based Medicinal Products as well as working in a GMP Cell Therapy Clinical Centre/Unit. Experience in Clinical Manufacturing of CAR T cells, NK cells, as well as other forms of cell-based medicinal products.

  • The applicant should have experience in the Clinical Manufacturing of CAR T cells, NK cells, as well as various other forms of cell-based medicinal products.
  • The applicant. should have received training in different types of Cellular therapy Processes & Services
  • Training in Cleanroom Design and also Development
  • Knowledge & training in all processes related to Chemistry Manufacturing and Records of CAR T cell therapy and other CBMPs as per International & national standards.
  • Experience in Validation, Quality Control, Quality Assurance of the cGMP based Cellular Processes.
  • Trained & experience in the regulatory framework for Cellular Therapies in India for Phase 1/11 Clinical Trials.
  • Experience with immunotherapies like CAR T cell therapy and also oncology-related cell types consisting of a subset of T cells, NK cells, macrophages, VSTs
  • The candidate should have experience on working with GMP grade closed automated Cell processing Equipment’s like Clinimax, Prodigy, Sepax, Xuri etc

Preferred:

  • Knowledge of all cGMP regulations and also FDA/EU/GTP guidance applicable to Biologics and also Cell Therapy manufacturing- Handling human-derived materials in ISO7/ISO8 cleanroom facility, cell expansion and also automated cell processing equipment
  • Experience in Cleanroom (ISO 7, ISO 8) design, workflow, validation & maintenance procedures based on Schedule Y COSCO standards.
  • Trained in manufacturing of autologous CAR-T products for clinical trials as well as a commercial operation in a controlled cGMP cleanroom environment.
  • Experience in handling Quality aspects of cell manufacturing, Manufacturing and Controls (CMG) sections, including response to regulatory &. IEC inquiries.
  • Experience in processing Environmental monitoring as well as in house qualification/ validation activities,
  • Experience in execution of the necessary Global Operating.
  • Procedures (GOPs), Standard Operating Procedures (SOPs) as well as Aseptic Techniques, Gowning.
  • Qualifications and various other relevant training.
  • Experience in Designing and optimizing validation tools for Stability testing, Release criteria.Testing as well as Quality Testing.
  • Experience in handling Leukapheresis Protocols & Cryopreservation of cellular immunotherapy products.
  • Experience in the upkeep of Batch record in line with GMP requirements.
  • Experience in developing, reviewing as well as managing amendments to the protocol, patient information sheet and study documentation and timely submission to IEC and Financing agency as per requirement.
  • Experience in Developing brand-new Clinical Trail protocol with investigators for regulatory and ethics committee submission (ICF,
  • IB, CRFs, Study forms) as well as CTRI registration of trial for brand-new Cell Therapy Products.

Desirable:

  • Conceive as well as develop novel in vitro assays/models to evaluate cell therapy efficacy in the context of the tumour microenvironment.
  • Project leadership across multiple projects/roles in a matrixed environment and also obtaining alignment across various functional groups to drive decision making.
  • Anticipate the need for contingencies as well as demonstrate flexibility with the development of alternative strategies.

Consolidated Salary: Rs. 67,700/- – Rs. 78,500/- p.m depending upon post- PhD experience.

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